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X-Wing Sliding Base

FDA UDI

Class I (US FDA UDI)

by Enztec Limited

Identity

Trade Name
X-Wing Sliding Base FDA UDI
Generic Name
Orthopaedic graft tensioner, reusable FDA UDI
Device Name
Intended to be used for the preparation and pre-tensioning of single tendon grafts for ligament reconstruction FDA UDI
Model / Reference
72205272 FDA UDI
Description
Intended to be used for the preparation and pre-tensioning of single tendon grafts for ligament reconstruction FDA UDI

Identifiers

Catalog Number
72205272 FDA UDI
Primary DI / UDI-DI
09421028113465 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic graft tensioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic graft tensioner, reusable

X-Wing Sliding Base by Enztec Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic graft tensioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Enztec Limited

Sources (1)

  • FDA UDI c25c5a11-0825-4aab-80ea-38fb72f62ce6 34 fields · synced May 30, 2026